A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550204



Internal ID15990927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22313047..22327341hg38UCSC Ensembl
Innerchr10:22601976..22616270hg19UCSC Ensembl
Innerchr10:22641982..22656276hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3814295
hg1914295
hg1814295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1002n54
Supporting Variantsnssv744705
Samples
Known GenesBMI1, COMMD3, COMMD3-BMI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550204
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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